PT  - JOURNAL ARTICLE
AU  - Madhusudhan Budatha
AU  - Jiasheng Zhang
AU  - Martin A. Schwartz
TI  - Fibronectin-mediated inflammatory signaling through integrin α5 in vascular remodeling
AID  - 10.1101/2021.01.06.425577
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.01.06.425577
4099  - http://biorxiv.org/content/early/2021/01/08/2021.01.06.425577.short
4100  - http://biorxiv.org/content/early/2021/01/08/2021.01.06.425577.full
AB  - Adhesion of vascular endothelial cells (ECs) to the underlying basement membrane potently modulates EC inflammatory activation. The normal basement membrane proteins laminin and collagen IV attenuate inflammatory signaling in part through integrin α2β1. In contrast, fibronectin, the provisional matrix protein found in injured, remodeling or inflamed vessels, sensitizes ECs to inflammatory stimuli through integrins α5β1and and αvβ3. A chimeric integrin in which the cytoplasmic domain of α5 is replaced with that of α2 pairs with β1 and binds fibronectin but signals like α2β1. Here, we examined mice in which integrin α5 is replaced with the α5/2 chimera, using the transverse aortic constriction (TAC) and partial carotid ligation (PCL) models of vessel remodeling. Following TAC and PCL surgery, WT mice showed increased fibronectin deposition and expression of inflammatory markers, which were strongly attenuated in a5/2 mice. α5/2 mice also showed reduced artery wall hypertrophy in the TAC model and diminished inward remodeling in the PCL model. Acute atherosclerosis after PCL in hyperlipidemic ApoE−/− mice on a high fat diet was dramatically decreased in α5/2 mice. These results underscore the key role for integrin α5 signaling in pathological vascular remodeling and support its potential as a therapeutic target.Competing Interest StatementThe authors have declared no competing interest.